NDC 63083-2122 Urinary Tract Drops 2122
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2122?
What are the uses for Urinary Tract Drops 2122?
Which are Urinary Tract Drops 2122 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CRATEVA MAGNA BARK (UNII: RS704ZO5ZL)
- CRATEVA MAGNA BARK (UNII: RS704ZO5ZL) (Active Moiety)
- AGATHOSMA BETULINA LEAF (UNII: 369DDH39Z0)
- AGATHOSMA BETULINA LEAF (UNII: 369DDH39Z0) (Active Moiety)
- SUS SCROFA URINARY BLADDER (UNII: 3G7U72W8DA)
- SUS SCROFA URINARY BLADDER (UNII: 3G7U72W8DA) (Active Moiety)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (Active Moiety)
- BEEF KIDNEY (UNII: 5HOC10FSIC)
- BEEF KIDNEY (UNII: 5HOC10FSIC) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- CHIMAPHILA UMBELLATA WHOLE (UNII: WCK21A9W9J)
- CHIMAPHILA UMBELLATA WHOLE (UNII: WCK21A9W9J) (Active Moiety)
- URTICA URENS WHOLE (UNII: IHN2NQ5OF9)
- URTICA URENS WHOLE (UNII: IHN2NQ5OF9) (Active Moiety)
Which are Urinary Tract Drops 2122 Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".